Transition Metal Complexes and Photodynamic Therapy from a Tumor-Centered Approach: Challenges, Opportunities, and Highlights from the Development of TLD1433

Susan Monro, Katsuya L. Colón, Huimin Yin, John Roque, Prathyusha Konda, Shashi Gujar, Randolph P. Thummel, Lothar Lilge, Colin G. Cameron, Sherri A. McFarland

Résultat de recherche: Review articleexamen par les pairs

1091 Citations (Scopus)

Résumé

Transition metal complexes are of increasing interest as photosensitizers in photodynamic therapy (PDT) and, more recently, for photochemotherapy (PCT). In recent years, Ru(II) polypyridyl complexes have emerged as promising systems for both PDT and PCT. Their rich photochemical and photophysical properties derive from a variety of excited-state electronic configurations accessible with visible and near-infrared light, and these properties can be exploited for both energy- and electron-transfer processes that can yield highly potent oxygen-dependent and/or oxygen-independent photobiological activity. Selected examples highlight the use of rational design in coordination chemistry to control the lowest-energy triplet excited-state configurations for eliciting a particular type of photoreactivity for PDT and/or PCT effects. These principles are also discussed in the context of the development of TLD1433, the first Ru(II)-based photosensitizer for PDT to enter a human clinical trial. The design of TLD1433 arose from a tumor-centered approach, as part of a complete PDT package that includes the light component and the protocol for treating non-muscle invasive bladder cancer. Briefly, this review summarizes the challenges to bringing PDT into mainstream cancer therapy. It considers the chemical and photophysical solutions that transition metal complexes offer, and it puts into context the multidisciplinary effort needed to bring a new drug to clinical trial.

Langue d'origineEnglish
Pages (de-à)797-828
Nombre de pages32
JournalChemical Reviews
Volume119
Numéro de publication2
DOI
Statut de publicationPublished - janv. 23 2019

Note bibliographique

Funding Information:
S.A.M., C.G.C., R.P.T., and S.G. thank the National Cancer Institute (NCI) of the National Institutes of Health (NIH) (Award R01CA222227) for support. The content in this review is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. S.A.M. and S.G. thank the Canadian Institutes of Health Research (CIHR), the Beatrice Hunter Cancer Research Institute (BHCRI), and the Dalhousie Medical Research Foundation (DMRF) for support. S.A.M. also acknowledges Theralase Technologies, Inc. (TLT) and the Natural Sciences and Engineering Council of Canada (NSERC), the Canadian Foundation for Innovation (CFI), the Nova Scotia Research and Innovation Trust (NSRIT), Acadia University, and the University of North Carolina at Greensboro for support. R.P.T. thanks the U.S. Department of Energy, Office of Science, and Office of Basic Energy Sciences under Award DE-FG02-07ER15888 as well as the Robert A. Welch Foundation (Grant E-621) for support.

Funding Information:
*E-mail cgcamero@uncg.edu (C.G.C.). *E-mail: samcfarl@uncg.edu (S.A.M.). ORCID Shashi Gujar: 0000-0002-5427-0829 Randolph P. Thummel: 0000-0001-9586-786X Lothar Lilge: 0000-0001-5533-0005 Colin G. Cameron: 0000-0003-0978-0894 Sherri A. McFarland: 0000-0002-8028-5055 Notes The authors declare the following competing financial interest(s): S.A.M. has received financial support from Theralase Technologies, Inc. (TLT). L.L. is a scientific consultant for Theralase Technologies, Inc. (TLT).

Publisher Copyright:
© 2018 American Chemical Society.

ASJC Scopus Subject Areas

  • General Chemistry

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